ABSTRACT
La dermatitis atópica es la forma más frecuente de eccema durante el primer año de vida; sin embargo, cuando la presentación es atípica o se asocia a infecciones, constituye un desafío diagnóstico para el pediatra. Es importante mantener un índice alto de sospecha para detectar inmunodeficiencias primarias asociadas a eccemas graves desde el período neonatal. Un ejemplo de estas es el síndrome de hiperinmunoglobulinemia E (hiper-IgE) autosómico dominante. Este cuadro se caracteriza por la presencia de infecciones cutáneas y respiratorias recurrentes, dermatitis atópica, eosinofilia y aumento de IgE. Se reporta el caso clínico de una niña de 1 mes y 29 días con diagnóstico de hiper-IgE con afección cutánea desde el nacimiento.
Atopic dermatitis is the most common form of eczema often developed before the first year of life. Nevertheless, when the presentation is atypical or related to infections the diagnostic represents a challenge for the pediatricians. It is important to maintain a high index of suspicion for the detection of primary immunodeficiency associated to severe eczema. One of them is the autosomal dominant hyper-IgE syndrome characterized by recurrent skin and respiratory infections, atopic dermatitis, eosinophilia, and high serum IgE concentrations. In this paper, we report a 1 months and 29 days old baby girl diagnosed with hyper-IgE and a skin involvement since birth.
Subject(s)
Humans , Female , Infant , Dermatitis, Atopic/diagnosis , Job Syndrome/diagnosis , Dermatitis, Atopic/immunology , Eczema/diagnosis , Eczema/immunology , Job Syndrome/complicationsABSTRACT
Objective. To explore the prevalence of common food and aeroallergens sensitization in early childhood skin diseases and to compare the pattern of common food and aeroallergens sensitization before and after 6 months among infants with atopic dermatitis (AD). Methods. All skin prick tests (SPTs) performed on children =< 18 months of age managed at the pediatric dermatology clinic of an university-affiliated teaching hospital over a 16-month period were examined. Results. There was generally no difference in the pattern of sensitization to common food and aeroallergens between AD patients and non-AD young children with miscellaneous dermatological or gastrointestinal conditions. Dust mites were the only common aeroallergens in these patients; whereas egg and peanuts were the common sensitizing food allergens. Cat and dog fur as aeroallergens, soy bean, orange and beef as food allergens were relatively uncommon among the studied subjects. In AD, infants =< 6 months were generally naive to aeroallergens but became sensitized to the D. Pteronyssinus in the next 12 months of age. 80% of these infants were not sensitized to cow’s milk and none sensitized to soybean. Conclusions. Atopic sensitization to common allergens was common in early childhood with or without AD. Majority of young infants were not sensitized to milk, and develop eczema before they show atopy to the milk or soy allergens.
Subject(s)
Animals , Arachis/immunology , Chi-Square Distribution , Eczema/immunology , Egg Hypersensitivity/immunology , Female , Food Hypersensitivity/immunology , Humans , Infant , Infant, Newborn , Male , Mites/immunology , Skin TestsSubject(s)
Humans , Male , Female , Eczema/immunology , Biopsy , Skin/pathology , Immunohistochemistry , Skin/anatomy & histology , Histological TechniquesABSTRACT
El síndrome de hiper IgE (SHIE) es una rara entidad que se caracteriza por presentar infecciones cutáneas y respiratorias, sobre todo neumonías a estafilococo, con posterior formación de neumatoceles, disturbios en el metabolismo óseo y una IgE sumamente elevada. En el presente artículo se trata de actualizar el tema en sus aspectos fisiopatológicos, inmunológicos y nuevas conductas de tratamiento
Subject(s)
Humans , Eosinophilia/physiopathology , Hypergammaglobulinemia/immunology , Immunoglobulin E/immunology , Job Syndrome/physiopathology , Eczema/etiology , Eczema/immunology , Eosinophilia/complications , Eosinophilia/immunology , Histamine/blood , Interferon Type I/deficiency , Interferon-gamma/deficiency , Interferon-gamma/therapeutic use , Osteogenesis Imperfecta/etiology , Osteoporosis/etiology , Job Syndrome/immunology , Job Syndrome/therapy , T-Lymphocytes/immunologyABSTRACT
Se presenta un caso de Reticuloide actínico, en un hombre de 52 años, de 10 años de evolución. Se estudió la población linfocitaria T a nivel sérico a través de anticuerpos monoclonales y la presencia de inmunocomplejos circulantes. Se discuten las distintas terapéuticas existentes y la escasa respuesta obtenida